A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587384



Internal ID16028107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33321856..33324197hg38UCSC Ensembl
Innerchr21:34694161..34696502hg19UCSC Ensembl
Innerchr21:33616031..33618372hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg382342
hg192342
hg182342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7817n54
Supporting Variantsnssv946630
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587384
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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